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FDA ANDA · ANDA077035

CITALOPRAM HYDROBROMIDE

Sponsor: FOSUN PHARMA

APPLICATION
ANDA077035
TYPE
ANDA
ORIGINAL APPROVAL
2004-10-28
LATEST ACTION
2024-11-25
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 20MG BASE · TABLET · ORAL
CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 40MG BASE · TABLET · ORAL
CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 10MG BASE · TABLET · ORAL

Approval history

2024-11-25Labeling · Supplement 12 · standardAP
2024-11-25Labeling · Supplement 13 · standardAP
2013-03-28Labeling · Supplement 11 · standardAP
2012-12-18Labeling · Supplement 10 · standardAP
2009-09-28Labeling · Supplement 9AP
2007-10-19Labeling · Supplement 8AP
2007-10-19Labeling · Supplement 6AP
2005-08-01Labeling · Supplement 5AP
2005-05-11Labeling · Supplement 4AP
2004-10-28OriginalLetterAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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